34322-78-6 Usage
Description
1-(3-methoxyphenyl)propan-2-ol, also known as isovanillyl alcohol, is a chemical compound with the molecular formula C10H14O2. It is a colorless liquid with a pleasant odor and is commonly used in the production of perfumes and fragrances. This secondary alcohol is derived from the phenylpropanoid pathway in plants and is also found in certain essential oils. Identified as a natural flavoring substance in the food industry, isovanillyl alcohol has been studied for its potential antioxidant and anti-inflammatory properties, making it of interest in medicinal and cosmetic chemistry. Furthermore, it has been investigated for its potential role in cancer prevention and treatment due to its ability to inhibit the growth of cancer cells.
Uses
Used in Perfumery and Fragrance Industry:
1-(3-methoxyphenyl)propan-2-ol is used as a key component in the creation of perfumes and fragrances for its pleasant odor and ability to enhance the overall scent profile of a product.
Used in Flavor and Food Industry:
As a natural flavoring substance, 1-(3-methoxyphenyl)propan-2-ol is used to add unique and desirable flavors to the food products, contributing to their overall taste and appeal.
Used in Medicinal Chemistry:
1-(3-methoxyphenyl)propan-2-ol is used as a potential therapeutic agent for its antioxidant and anti-inflammatory properties, which may help in the development of treatments for various health conditions.
Used in Cosmetic Chemistry:
1-(3-methoxyphenyl)propan-2-ol is used in the development of cosmetic products due to its potential antioxidant and anti-inflammatory properties, which can contribute to the skincare and beauty industry by providing beneficial effects to the users.
Used in Cancer Research and Treatment:
1-(3-methoxyphenyl)propan-2-ol is used as a compound of interest in cancer research, particularly for its potential role in cancer prevention and treatment. Its ability to inhibit the growth of cancer cells makes it a promising candidate for further study and development in the field of oncology.
Check Digit Verification of cas no
The CAS Registry Mumber 34322-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,2 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34322-78:
(7*3)+(6*4)+(5*3)+(4*2)+(3*2)+(2*7)+(1*8)=96
96 % 10 = 6
So 34322-78-6 is a valid CAS Registry Number.
34322-78-6Relevant articles and documents
A 3 - (2 - amino-propyl) phenol preparation method (by machine translation)
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Paragraph 0032; 0033; 0034; 0035; 0036; 0049; 0050; 0064, (2017/08/28)
The invention discloses a 3 - (2 - amino-propyl) phenol preparation method, in order to methoxy bromophenylacetic, epoxy propane, methyl sulfonic acid, ammonia methanol and hydrobromic acid as the raw materials, through the four-step reaction to obtain the target product 3 - (2 - amino-propyl) phenol. The invention has simple operation, environment friendly, comprehensive yield is 63% more, than the existing 35.6% yield, with a remarkable enhancement, greatly reduces the production cost of the existing drugs, is suitable for industrial scale production. (by machine translation)
Chemoenzymatic synthesis of enantiomerically pure syn-configured 1-aryl-3-methylisochroman derivatives
Simon, Robert C.,Busto, Eduardo,Richter, Nina,Belaj, Ferdinand,Kroutil, Wolfgang
, p. 111 - 121 (2014/01/06)
A two-step synthesis of various enantiomerically pure 1-aryl-3- methylisochroman derivatives was accomplished through asymmetric biocatalytic ketone reduction followed by an oxa-Pictet-Spengler reaction. The compounds were obtained in good to excellent yield (47-92 %) in favor of the syn diastereomers [dr (syn/anti) up to 99:1]. Enantiopure arylpropanols serving as pronucleophiles for the C-C bond-formation step were obtained by biocatalytic reduction by employing enantiocomplementary alcohol dehydrogenases, which gave access to the (S) and (R) enantiomer with up to >99 % conversion and up to >99 % ee. A two-step sequence involving a biocatalytic hydrogen-transfer reduction and a syn-diastereoselective oxa-Pictet-Spengler reaction was established to provide a series of 1-aryl-3-methylchroman derivatives with perfect enantioselectivity; PTSA = para-toluenesulfonic acid. Copyright
Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst
Li, Gang,Leow, Dasheng,Wan, Li,Yu, Jin-Quan
supporting information, p. 1245 - 1247 (2013/03/13)
Weak coordination is powerful! A PdII-catalyzed olefination of ortho-C-H bonds of arenes directed by weakly coordinating ethers is developed by using monoprotected amino acid (MPAA) ligands. This finding provides a method for chemically modifying ethers, which are abundant in natural products and drug molecules. HFIP=hexafluoroisopropanol. Copyright
